| Distance: | Resume alert | Resumes 401 - 410 of 641 |
Engineering Design
Potomac, MD
... Realized and participated in a full development cycle from initial concept phase through risk assessment, feasibility, planning, design, and development to pre-market FDA submission. Designed and developed real time embedded firmware for the POC-5LP ... - 2016 Dec 27
... Realized and participated in a full development cycle from initial concept phase through risk assessment, feasibility, planning, design, and development to pre-market FDA submission. Designed and developed real time embedded firmware for the POC-5LP ... - 2016 Dec 27
Mechanical Engineering Medical
Kensington, MD, 20895
... Skills Summary Product R&D/Product Development Medical Diagnostics/Medical Devices Line Management Project Management Design Controls (FDA 21 CFR 820, ISO 9000, ISO 13485) Engineering Mechanical Engineering Opto-mechanical & Optical Engineering ... - 2016 Dec 21
... Skills Summary Product R&D/Product Development Medical Diagnostics/Medical Devices Line Management Project Management Design Controls (FDA 21 CFR 820, ISO 9000, ISO 13485) Engineering Mechanical Engineering Opto-mechanical & Optical Engineering ... - 2016 Dec 21
Research Associate
Rockville, MD
... May-Nov 2012 Research position at the FDA in Rockville MD- Job duties: Development and characterization of novel vaccines against the most virulent types of Malaria in sub-Saharan Africa. Assisted in DNA cloning, restriction digestion, plasmid preps ... - 2016 Dec 11
... May-Nov 2012 Research position at the FDA in Rockville MD- Job duties: Development and characterization of novel vaccines against the most virulent types of Malaria in sub-Saharan Africa. Assisted in DNA cloning, restriction digestion, plasmid preps ... - 2016 Dec 11
Professional Experience Microsoft Office
Washington, DC
... Assisted in the check and verification process of hard copy materials and the integrity of FDA DARRTS database. Enhanced and improved the efficiency of processing activities performed in the document room. Provided input concerning document room ... - 2016 Nov 27
... Assisted in the check and verification process of hard copy materials and the integrity of FDA DARRTS database. Enhanced and improved the efficiency of processing activities performed in the document room. Provided input concerning document room ... - 2016 Nov 27
Sales Management
Bethesda, MD
... staff of 50+ handling client operations, account management, sales, product management, and support for licensing agreements, FDA cGMP manufacturing, and 3rd-party lab testing Led several successful projects on Government Eligibility Screening, e ... - 2016 Oct 17
... staff of 50+ handling client operations, account management, sales, product management, and support for licensing agreements, FDA cGMP manufacturing, and 3rd-party lab testing Led several successful projects on Government Eligibility Screening, e ... - 2016 Oct 17
Safety Manager
Hyattsville, MD
... Upon receipt of guidance from the FDA, researched and generated text material on medical devices Follow up on all product recalls used in conjunction with patient care Notified Worker’s Compensation /Board for employees returning to work program ... - 2016 Sep 29
... Upon receipt of guidance from the FDA, researched and generated text material on medical devices Follow up on all product recalls used in conjunction with patient care Notified Worker’s Compensation /Board for employees returning to work program ... - 2016 Sep 29
Administrative Assistant Microsoft Office
Fairfax, VA
... of FDA) Fairfax, VA OPM Level 5 Clearance Provides quality assurance of entered data and the critical feedback to staff using a database designed to capture, track, and report errors. Performs and resolves problems related to government generated ... - 2016 Aug 19
... of FDA) Fairfax, VA OPM Level 5 Clearance Provides quality assurance of entered data and the critical feedback to staff using a database designed to capture, track, and report errors. Performs and resolves problems related to government generated ... - 2016 Aug 19
Quality Control
Ashburn, VA
... and vendor quality auditing to ISO 13485 / 21 CFR Part 820 Performing final release of product before shipment Provide support for FDA, CSA and UL audits Responsible for applying LEAN manufacturing techniques to the production lines BAYER HEALTHCARE ... - 2016 Aug 16
... and vendor quality auditing to ISO 13485 / 21 CFR Part 820 Performing final release of product before shipment Provide support for FDA, CSA and UL audits Responsible for applying LEAN manufacturing techniques to the production lines BAYER HEALTHCARE ... - 2016 Aug 16
Medical Development
Chantilly, VA
... Managed group projects for researching and developing FDA-approved diagnostic kits for automated immunoassay, led multiple projects simultaneously, oversaw scientific and technical parts of FDA submissions, and provided support for new product ... - 2016 Aug 09
... Managed group projects for researching and developing FDA-approved diagnostic kits for automated immunoassay, led multiple projects simultaneously, oversaw scientific and technical parts of FDA submissions, and provided support for new product ... - 2016 Aug 09
Purchasing Specialist
Ashburn, VA
... Locate data in multiple source systems including FDA Website and SharePoint Work independently on Excel worksheets (Single Template Spreadsheets) as provided by Data Mining Team Lead. Collect and report attribute data associated with a specific sku ... - 2016 Jul 24
... Locate data in multiple source systems including FDA Website and SharePoint Work independently on Excel worksheets (Single Template Spreadsheets) as provided by Data Mining Team Lead. Collect and report attribute data associated with a specific sku ... - 2016 Jul 24